Messana, T., Russo, A., Vergaro, R., Boni, A., Santucci, M., & Pini, A. (2018). Glucose Transporter Type 1 Deficiency Syndrome: Developmental Delay and Early-Onset Ataxia in a Novel Mutation of the SLC2A1 Gene. J Pediatr Neurosci.
Citación estilo ChicagoMessana, Tullio, Angelo Russo, Raffaella Vergaro, Antonella Boni, Margherita Santucci, and Antonella Pini. "Glucose Transporter Type 1 Deficiency Syndrome: Developmental Delay and Early-Onset Ataxia in a Novel Mutation of the SLC2A1 Gene." J Pediatr Neurosci 2018.
Cita MLAMessana, Tullio, et al. "Glucose Transporter Type 1 Deficiency Syndrome: Developmental Delay and Early-Onset Ataxia in a Novel Mutation of the SLC2A1 Gene." J Pediatr Neurosci 2018.
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